About   Help   FAQ
Disease Ontology Browser
hereditary sensory and autonomic neuropathy type 1A (DOID:0070152)
Alliance: disease page
Synonyms: hereditary sensory and autonomic neuropathy type IA; hereditary sensory neuropathy type 1A; hereditary sensory neuropathy type IA; HSAN1A; HSN1A
Alt IDs: OMIM:162400, UMLS_CUI:C5235211
Definition: A hereditary sensory and autonomic neuropathy type 1 characterized by onset of sensorimotor axonal neuropathy in the first or second decades of life that has_material_basis_in heterozygous mutation in the SPTLC1 gene on chromosome 9q22.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/14/2026
MGI 6.24
The Jackson Laboratory